DC44SMe | MCEDC44SMe, a phosphate proagent of cytotoxic DNA alkylator DC44, can ...

NF546 | MCENF546 is a selective non-nucleotide bP2Y11/b agonist with a bpECsub50...

BAY-1797 | MCEBAY-1797 is a potent, orally active, and selective bP2X4/b antagon...

PROTAC ER Degrader-4 | MCEPROTAC ER Degrader-4 is a bvon Hippel-Lindau/b-based b...

(rel)-PROTAC ERRα Degrader-1 | MCE(rel)-PROTAC ERRα Degrader-1 is a relative con...

Aβ42-IN-1 | MCEAβ42-IN-1, compound1v, is a novel, potent and orally activebγ-sec...

(S)-GNE-987 | MCE(S)-GNE-987 (compound 4), the GNE-987 (a chimeric BET degrader)...

M-525 | MCEM-525 is a fit-in-class, highly potent, irreveible and covalent bmeni...

K-Ras ligand-Linker Conjugate 2 | MCEK-Ras ligand-Linker Conjugate 2 incorporate...

TT-OAD2 free base | MCETT-OAD2 free base is a non-peptide bglucagon-like peptide...

Thalidomide-NH-C6-NH2 | MCEThalidomide-NH-C6-NH2 is a synthesized bE3 ligase lig...

Thalidomide-PEG2-C2-NH2 | MCEThalidomide-PEG2-C2-NH2 is a synthesized bE3 ligase...

Mcl-1 antagonist 1 | MCEMcl-1 antagonist 1 is a bMcl-1/b protein antagonist extr...

BAY-298 | MCEBAY-298 is an orally active and selective bluteinizing hormone rece...

JHU395 | MCEJHU395 is an orally-bioavailable and a plasma stable lipophilic bglu...

KDOAM-25 citrate | MCEKDOAM-25 citrate is a potent and highly selective bhistone...

(Rac)-VU 6008667 | MCE(Rac)-VU 6008667 is a selective negative allosteric modula...

CLZ-8 | MCECLZ-8 (Compound 8) is an orally active bMcl-1-PUMA/b interface inhibi...

MC-Val-Cit-PAB-rifabutin | MCEMC-Val-Cit-PAB-rifabutin is a bagent-linker conjug...

Tecarfarin sodium | MCETecarfarin sodium (ATI-5923 sodium) is a novel orally act...